BIOL 1D: INTRODUCTION TO MOLECULAR GENETICS
Foothill College Course Outline of Record
Heading | Value |
---|---|
Effective Term: | Summer 2023 |
Units: | 4 |
Hours: | 4 lecture per week (48 total per quarter) |
Prerequisite: | BIOL 1A. |
Advisory: | Students taking the biology majors' sequence (BIOL 1A, 1B, 1C, 1D) are strongly advised to take the sequence in order and in its entirety. |
Degree & Credit Status: | Degree-Applicable Credit Course |
Foothill GE: | Non-GE |
Transferable: | CSU/UC |
Grade Type: | Letter Grade (Request for Pass/No Pass) |
Repeatability: | Not Repeatable |
Student Learning Outcomes
- Explain the relationship between structure and function as observed in key enzymes used in DNA replication, transcription and translation.
- Demonstrate an understanding of how experimental evidence is used to draw conclusions regarding the structure and function of important genetic molecules.
- Demonstrate the ability to examine current scientific literature, and draw conclusions based on published current research
- Demonstrate the ability to understand the link between DNA structure, and it's function as the molecule of heredity, and evolutionary change
Description
Course Objectives
The student will be able to:
- Explain the key experiments that led to the discovery of DNA structure and function
- Describe the role of genes within cells
- Discuss the evolution of the three domains: Archaea, Bacteria, and Eukarya
- Compare and contrast genome organization of prokaryotes and eukaryotes
- Describe the steps of DNA replication and explain the molecular basis for DNA replication's remarkable fidelity
- Compare and contrast prokaryotic and eukaryotic DNA polymerase and DNA replication
- Describe the various mechanisms that cause DNA damage and mutation
- Describe DNA repair systems, comparing and contrasting prokaryotic and eukaryotic systems
- Explain the mechanisms and importance of recombination, repair, and transposition
- Describe transcription in prokaryotes
- Describe transcription in eukaryotes
- Compare and contrast transcription and RNA processing in prokaryotes and eukaryotes
- Describe the various types of post-transcriptional processing
- Describe protein translation
- Compare and contrast control of gene expression in prokaryotes and eukaryotes
- Describe basic methods in molecular genetics and discuss their applications
- Describe some of the contributions made by eminent scientists, including women and minorities, to the fields of molecular and cell biology
- Critically read and discuss original scientific papers
- Explore and discuss scientific questions for which there is as yet no single, generally accepted answer
Course Content
- Brief history/Key experiments
- Experiments that identified DNA as the molecule of inheritance
- Discovery of the structure of DNA
- Experiments that led to our initial understanding of transcription
- Experiments that led to our initial understanding of translation
- Elucidation of the genetic code
- Molecular nature of genes
- Storing and using genetic information
- Replication
- Mutation
- Recombination
- Evolution of Archaea, Bacteria, and Eukarya
- Molecular evolution
- Conserved sequences
- Molecular clocks
- rRNA
- Histone genes
- Subunits of DNA polymerase
- Subunits of RNA polymerase
- Genome organization
- Prokaryotic
- Eukaryotic
- Nucleosomes and chromatin packaging into chromosomes
- Introns and exons
- Nonrepetitive DNA, moderately repetitive DNA, and highly repetitive DNA
- Gene clusters
- Organelle DNA: mitochondria and chloroplast
- DNA replication
- Replicons
- DNA structure and the primer:template junction
- Enzymes
- Helicase and helicase loader
- Single stranded binding proteins
- Topoisomerases
- Primase
- RNAse H
- Ligase
- Histone chaperones
- Sliding clamp and sliding clamp loaders
- DNA polymerase
- Three dimensional structure - palm, finger, and thumb domains
- Processivity
- Fidelity of replication (molecular basis of proof-reading function)
- Holoenzyme - catalytic core, tao, sliding clamp, clamp loader
- Initiation
- Elongation - trombone model
- Termination
- Regulation
- Prokaryotic and Eukaryotic replication
- Origins of replication - replicators and initiators
- DNA polymerases - similarities and differences
- Regulation - similarities and differences
- Mutation and DNA damage
- Types of mutation
- Estimating mutation rates
- Base pair modifications
- Tautomers
- Alkylation
- Deamination
- Depurination
- Oxidation
- Intercalating agents
- Base analogs
- UV radiation and dimers
- Ionizing radiation and chromosome breaks
- DNA repair systems
- Direct repair
- Mismatch repair
- Base excision repair
- Nucleotide excision repair
- Recombination
- Nonhomologous end joining
- Translesion synthesis
- Recombination and transposition
- Homologous recombination
- RecA protein
- Holliday junctions
- Meiotic recombination
- Transposition
- Transposons
- Retrotransposons
- Transposable elements in different genomes
- Transcription in prokaryotes
- Transcription overview and transcription bubbles
- Prokaryotic promoters
- Prokaryotic RNA polymerase
- Initiation, elongation, and termination
- Regulation of transcription
- Transcription in Eukaryotes
- Eukaryotic RNA polymerases
- Transcription factors
- TATA box binding protein
- Eukaryotic promoters
- Class I
- Class III
- Class II
- CTD tail and mediator complex
- Regulation of transcription
- Prokaryotic and Eukaryotic transcription
- RNA polymerases
- RNA processing
- Post-transcriptional processing
- 5' cap
- Poly A tail
- Splicing
- Spliceosome
- Splicing reactions
- Splicing errors
- Alternative splicing
- Translation
- Ribosomes, messenger RNA, and transfer RNA
- The genetic code
- Initiation
- Elongation
- Termination
- Protein structure and localization
- Regulation of gene expression
- Negative and positive control
- Operons
- Eukaryotic regulation
- Chromatin modification
- Control elements and transcription factors
- Enhancers and activators
- Post-transcriptional regulation
- Nondcoding RNAs
- MicroRNAs
- Small interfering RNAs
- Chromatin remodeling and silencing
- Laboratory methods (description and discussion only)
- Tools for recombinant DNA technology
- Vectors
- Restriction enzymes
- Ligase
- Cloning
- Selected applications
- Centrifugation and Svedberg units
- Melting curves and C0t curves
- Electrophoresis
- DNA fingerprints
- DNA footprints
- Tools for recombinant DNA technology
Lab Content
Not applicable.
Special Facilities and/or Equipment
2. Students need internet access
Method(s) of Evaluation
One or more objective written midterm exams
Frequent quizzes that include both short answer and objective questions
In-class activities involving evaluation of current relevant scientific articles
Written objective comprehensive final exam
Method(s) of Instruction
Lecture presentations
Classroom discussions on relevant scientific articles
Guided group/collaborative activities on required readings and relevant scientific articles
Representative Text(s) and Other Materials
Urry, L.A., et al.. Campbell Biology, 12th ed.. 2021.
Supplemental text:
Krebs, Jocelyn E., Elliott S. Goldstein, and Stephen T. Kilpatrick. Lewin's Genes XII. 2018.
Types and/or Examples of Required Reading, Writing, and Outside of Class Assignments
- Reading assignments:
- Weekly reading assignments from primary text and assigned relevant scientific articles
- Supplemental reading assignments from web sources relevant to course material
- Writing assignments:
- Weekly assignment to answer objective set questions and define vocabulary
- Participation in class discussions of scientific articles
- Computation:
- Construct and interpret graphs
- Interpret melting curves and C0t curves
- Interpret DNA footprint and DNA fingerprint data
- Calculate and interpret recombination frequencies
- Interpret laboratory data from relevant key experiments in the field of molecular genetics